Formation of y + 10 and y + 11 ions in the collision-induced dissociation of peptide ions

Abstract

Tandem mass spectra of peptide ions, acquired in shotgun proteomic studies of selected proteins, tissues, and organisms, commonly include prominent peaks that cannot be assigned to the known fragmentation product ions (y, b, a, neutral losses). In many cases these persist even when creating consensus spectra for inclusion in spectral libraries, where it is important to determine whether these peaks represent new fragmentation paths or arise from impurities. Using spectra from libraries and synthesized peptides, we investigate a class of fragment ions corresponding to y n-1+10 and y n-1+ 11, where n is the number of amino acid residues in the peptide. These 10 and 11 Da differences in mass of the y ion were ascribed before to the masses of [+ CO - H 2O] and [+ CO - NH 3], respectively. The mechanism is suggested to involve dissociation of the N-terminal residue at the CH-CO bond following loss of H 2O or NH 3. MS 3 spectra of these ions show that the location of the additional 10 or 11 Da is at the N-terminal residue. The y n-1+10 ion is most often found in peptides with N-terminal proline, asparagine, and histidine, and also with serine and threonine in the adjacent position. The y n-1+11 ion is observed predominantlywith histidine and asparagine at the N-terminus, but also occurs with asparagine in positions two through four. The intensities of the y n-1+10 ions decrease with increasing peptide length. These data for y n-1+10 and y n-1+11 ion formation may be used to improve peptide identification from tandem mass spectra. ©2011 American Society for Mass Spectrometry (outside the USA).